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Concentration starting

The upstream concentration starts at and ends at as described by the following relationship ... [Pg.298]

Subsequently, after about 400 s the nitrogen concentration starts to decrease and, at the same time, evolution of hydrogen in the gas phase and formation of ammonia were observed. Ammonia is by far the most important by-product of the reduction of NO adsorbed species over LNT systems, as also reported by several authors [11,27,50,51],... [Pg.192]

As natural biological attenuation occurs, the rate of degradation of the contaminants in the soil can be estimated by calculating their half-lives. At the end of each half-life period, the concentration of the contaminant will be reduced by one half. Beginning with a concentration starting time 0, the sequence then is 1 /2, lU, /8,. .. for each succeeding half-life time period assuming all processes continue uninterrupted. [Pg.404]

The third possibility refers to a set of research topics on the development of methods making possible to estimate on-line — for control or diagnosis purposes — the input process concentrations. Starting from the knowledge... [Pg.130]

The median sulphate reduction rate is —0.89 peq yr The decrease of sulphate concentrations started at the beginning of the 1980s, quickly after the beginning of the improvement of the air sulphur oxide concentrations, suggesting a fast chemical response of the lakes. The thin soil and the relatively small sulphur storage, typical for high altitudes, surely contributed to the rapid response in most of the studied lakes. [Pg.131]

Stationary flow does not necessarily imply that the concentration of a chemical along the river is stationary as well. Often one has to assess the fate of chemicals that are accidentally spilled into a river and are transported downstream as a concentration cloud. It may be important to predict the temporal change of the concentration of the chemicals at a given location downstream of the spill, especially the time when the concentration starts to increase and when the maximum concentration of the spill passes by that location. [Pg.1102]

A linear increase in RNA concentration, starting at the moment when the RNA concentration becomes (approximately) equal to the enzyme concentration. [Pg.122]

I.I. Concentration gradient Across a Membrane. In the instance that a membrane separates two solutions of the same electrolyte, but with different concentrations F. Helfferich (ref. 55, page 319) calculated the ion-fluxes and the profiles of the internal concentrations, starting from the Nernst-Planck equations. Gradients of activity coefficients could be involved. However, convection (osmosis) had to be neglected. [Pg.323]

If the sulfide concentration in the sample is expected to be high or found to be high from qualitative testing, use methylene blue standard solution I. Otherwise, for a low concentration, use a diluted solution of this standard, methylene blue solution II. Add methylene blue solution(s) dropwise to tube B until the color matches to that developed in tube A. For high concentrations, start with dropwise addition of solution I. When the color is close to matching, add solution II dropwise. [Pg.256]

Figure 7.3 Calculated plots of Y versus [heme] -1/2 at five [02], expressed as molar concentrations. Starting at the top the oxygen conentrations are 10 4, 2xl0-5, 10-5, 5 x 10-6, and 10-6M. The intercepts give values of Yx. [Reprinted from R. A. Alberty, Biophys. Chem. 63, 119- 132 (1997), with permission from Elsevier Science.]... Figure 7.3 Calculated plots of Y versus [heme] -1/2 at five [02], expressed as molar concentrations. Starting at the top the oxygen conentrations are 10 4, 2xl0-5, 10-5, 5 x 10-6, and 10-6M. The intercepts give values of Yx. [Reprinted from R. A. Alberty, Biophys. Chem. 63, 119- 132 (1997), with permission from Elsevier Science.]...
Here Cp is the product concentration, Cp>max is the maximum product concentration when cell growth stops, and nP is the order of inhibition. At low values of Cp, the inhibition term plays no significant role. However, as the product concentration increases, the cell growth rate begins to decrease until the biomass concentration eventually reaches a plateau (what is called the stationary phase). From there, the fermentation broth is typically harvested before the cells start to die and the biomass concentration starts to decrease. [Pg.14]

Below the photic layer the nitrate concentrations start to increase, from the depth where nitrite and ammonia maxima are usually observed. In the regions affected by the coastal influx concentrations of inorganic nitrogen, compounds are larger and they may suddenly increase during the rains [45]. [Pg.287]

Methane forms microbiologically in strictly anaerobic conditions, but it is oxidized in both oxic and anoxic conditions [73]. The typical values for methane concentrations in the oxic layer are about 0.006-0.009 pM. The increase in methane concentration starts at erg = 15.92 kgm-3. At the onset of hydrogen sulfide, methane concentrations reach 0.350-0.500 pM. The vertical gradient of methane over the density range og = 16.20-16.40 kgm-3 is equal to 0.036-0.054 pMm-1. In the layer of a = 15.90-15.93 kgm-3 the methane... [Pg.292]

First, let us consider a situation in which the concentration starts at zero and goes up to a steady-state value. An example is a clean lake in which someone starts dumping some pollutant at a constant rate (perhaps the green dye mentioned above). Because the dumping just started, the flow of the pollutant into the lake is greater than its flow out of the lake, and the flow into the lake is constant. We know that the concentration at time = 0 is... [Pg.39]

Let us go back to the problem of the green dye dumped into Lake Kelly. Before the town fathers decided to dye the lake water green, the concentration of dye was zero. After they started dumping the dye into the lake, the concentration started to increase in fact, the concentrations (in ppm) measured every 6 months were 0.33, 0.50, 0.66, and 0.70. [Pg.53]

Luo and Ollis [204] compared the influence of water vapour on toluene with other compounds and found that the influence of water depended upon the characteristics of the contaminants. The research indicated that in a toluene-air mixture there was no toluene degradation in the absence of water, the toluene oxidation rate began to decrease when the water concentration started to reach saturation levels. Martra et al. [209] found that water vapour was needed to keep steady state toluene conversion to benzaldehyde and that in a dry toluene/air mixture an irreversible deactivation of the catalyst occurred. Their results further indicated that the produced benzaldehyde could undergo further oxidation but only in the presence of water. Kaneko and Okura [232] reported that the concentration of CO2 increased linearly with increases in the relative humidity and that the yield at 60% relative humidity was greater by one order than under dry conditions. The yield of benzaldehyde, however, decreased sharply with increased relative humidity and it was proposed that an increase in hydroxyl radicals may compete and/or hinder adsorption of toluene on the surface of Ti02 hence resulting in retardation of toluene oxidation. Kaneko and Okura [232], however, concluded that the effect of water vapour on the photocatalytic oxidation of toluene may depend on the initial pollutants concentration and its adsorptiv-ity. Pengyi et al. [234] observed that the effect of water vapour was two sided in that a little humidity can improve the decomposition of toluene whilst too much can suppress the decomposition. This was explained by the fact that hu-... [Pg.408]

Solution measurements the measurements are performed with different concentrations, starting preferably with the lowest and proceeding to the highest. [Pg.513]

We see from Figure 7-5 that for an initiator concentration 0.001 M, the monomer concentration starts at 3 M and levels off at a concentration of 0.6 M, corresponding to a maximum conversion of 80%. [Pg.201]

The underlying value dimension here might be called freedom. The Buddha taught that the ordinary state is one of suffering and entrapment in the forms and delusions of our own minds. The root cause of this suffering is attachment, the (automatized) desire to prolong pleasure and avoid pain. The journey along the Path of Concentration starts when the meditater tries to focus attention on some particular... [Pg.135]


See other pages where Concentration starting is mentioned: [Pg.151]    [Pg.211]    [Pg.619]    [Pg.249]    [Pg.460]    [Pg.187]    [Pg.969]    [Pg.162]    [Pg.198]    [Pg.187]    [Pg.117]    [Pg.432]    [Pg.72]    [Pg.169]    [Pg.37]    [Pg.176]    [Pg.230]    [Pg.43]    [Pg.291]    [Pg.226]    [Pg.93]    [Pg.123]    [Pg.128]    [Pg.291]    [Pg.211]    [Pg.553]    [Pg.85]    [Pg.1081]    [Pg.120]    [Pg.73]   


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INDEX starting concentration

Starting concentration profile, boundary layer

Substrate (Starting Material) Concentrations

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